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Ethanone, 1-cyclooctyl-, also known as 1-cyclooctylethanone or cyclooctanone, is an organic compound with the chemical formula C10H16O. It is a cyclic ketone, featuring an eight-membered cycloalkane ring with a carbonyl group (C=O) attached to one of the carbon atoms. Ethanone, 1-cyclooctyl- is a colorless liquid with a strong, pungent odor and is insoluble in water but soluble in organic solvents. Cyclooctanone is used as a synthetic intermediate in the production of various chemicals, pharmaceuticals, and fragrances. It is also employed as a solvent and a reagent in organic synthesis. Due to its cyclic structure and ketone functional group, it exhibits unique chemical properties and reactivity, making it a valuable compound in the field of organic chemistry.

6713-50-4

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6713-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6713-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,1 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6713-50:
(6*6)+(5*7)+(4*1)+(3*3)+(2*5)+(1*0)=94
94 % 10 = 4
So 6713-50-4 is a valid CAS Registry Number.

6713-50-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclooctylmethylketon

1.2 Other means of identification

Product number -
Other names cyclooctyl methyl ketone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6713-50-4 SDS

6713-50-4Relevant academic research and scientific papers

CYCLOOCT-(EN-)YL DERIVATIVES FOR USE AS FRAGRANCES

-

Page/Page column 12, (2008/06/13)

This invention relates to substituted cyclooctenes of formula (I), wherein X and R are defined in the specification.

Wanderungstendenzen cyclischer, polycyclischer und methylverzweigter Alkylreste bei der Beckmann-Umlagerung

Langhals, Heinz,Ruechardt, Christoph

, p. 3831 - 3854 (2007/10/02)

The migration aptitudes of polycyclic bridgehead groups, cycloalkyl groups as well as of β-, γ- and δ-branched alkyl groups in the Chapman variant of the Beckmann rearrangement were determined.From these data it is concluded that at transition state 2 the migrating group is not resembling a planarised carbenium ion R+, but rather a pentacoordinated carbonium ion structure.Because only small geometrical changes occur in the migrating group vertical stabilisation of charge at transition state is believed to have significant influence on the migration aptitudes.

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